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中文
通过CRISPR/Cas9基因编辑系统，对Lrba基因引入了14个碱基的缺失，导致Exon2中包含起始转录位点的区域产生了一个框移突变，进而导致LRBA蛋白部分缺失。(来源：J:332889)
Basic Information
Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
Phenotypes
Legend：
hm: homozygous
ht: heterozygous
cn: conditional genotype
cx: complex: > 1 genome feature
tg: involves transgenes
ot: other: hemizygous, indeterminate,...
(F): Female
(M): Male
phenotype observed
N: normal phenotype
(#): related diseases count
Phenotypes：
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| Phenotypes |
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References Literature
Title
PMID
Journal
Year
IF
